{"title":"Vaccination for communicable endemic diseases: optimal allocation of initial and booster vaccine doses.","authors":"Isabelle J Rao, Margaret L Brandeau","doi":"10.1007/s00285-024-02111-x","DOIUrl":null,"url":null,"abstract":"<p><p>For some communicable endemic diseases (e.g., influenza, COVID-19), vaccination is an effective means of preventing the spread of infection and reducing mortality, but must be augmented over time with vaccine booster doses. We consider the problem of optimally allocating a limited supply of vaccines over time between different subgroups of a population and between initial versus booster vaccine doses, allowing for multiple booster doses. We first consider an SIS model with interacting population groups and four different objectives: those of minimizing cumulative infections, deaths, life years lost, or quality-adjusted life years lost due to death. We solve the problem sequentially: for each time period, we approximate the system dynamics using Taylor series expansions, and reduce the problem to a piecewise linear convex optimization problem for which we derive intuitive closed-form solutions. We then extend the analysis to the case of an SEIS model. In both cases vaccines are allocated to groups based on their priority order until the vaccine supply is exhausted. Numerical simulations show that our analytical solutions achieve results that are close to optimal with objective function values significantly better than would be obtained using simple allocation rules such as allocation proportional to population group size. In addition to being accurate and interpretable, the solutions are easy to implement in practice. Interpretable models are particularly important in public health decision making.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11533358/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"100","ListUrlMain":"https://doi.org/10.1007/s00285-024-02111-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
Abstract
For some communicable endemic diseases (e.g., influenza, COVID-19), vaccination is an effective means of preventing the spread of infection and reducing mortality, but must be augmented over time with vaccine booster doses. We consider the problem of optimally allocating a limited supply of vaccines over time between different subgroups of a population and between initial versus booster vaccine doses, allowing for multiple booster doses. We first consider an SIS model with interacting population groups and four different objectives: those of minimizing cumulative infections, deaths, life years lost, or quality-adjusted life years lost due to death. We solve the problem sequentially: for each time period, we approximate the system dynamics using Taylor series expansions, and reduce the problem to a piecewise linear convex optimization problem for which we derive intuitive closed-form solutions. We then extend the analysis to the case of an SEIS model. In both cases vaccines are allocated to groups based on their priority order until the vaccine supply is exhausted. Numerical simulations show that our analytical solutions achieve results that are close to optimal with objective function values significantly better than would be obtained using simple allocation rules such as allocation proportional to population group size. In addition to being accurate and interpretable, the solutions are easy to implement in practice. Interpretable models are particularly important in public health decision making.
对于某些传染性地方病(如流感、COVID-19),接种疫苗是防止感染传播和降低死亡率的有效手段,但必须随着时间的推移使用疫苗加强剂量。我们考虑的问题是,如何在人口的不同亚群之间以及在初始剂量和加强剂量之间优化分配有限的疫苗供应,并允许多次加强剂量。我们首先考虑的是一个 SIS 模型,该模型具有相互影响的人群和四个不同的目标:最小化累积感染、死亡、寿命损失或因死亡而损失的质量调整寿命。我们按顺序解决问题:对于每个时间段,我们使用泰勒级数展开法近似系统动态,并将问题简化为片断线性凸优化问题,从而得出直观的闭式解。然后,我们将分析扩展到 SEIS 模型的情况。在这两种情况下,疫苗都是根据优先顺序分配给各组的,直到疫苗供应耗尽为止。数字模拟表明,我们的分析解决方案取得了接近最优的结果,其目标函数值大大优于使用简单的分配规则(如按群体规模比例分配)所取得的结果。除了准确和可解释之外,这些解决方案在实践中也很容易实施。可解释的模型在公共卫生决策中尤为重要。